LinkedIn

 آمار

تعداد نشریات20
تعداد شماره‌ها1,093
تعداد مقالات10,031
تعداد مشاهده مقاله27,616,076
تعداد دریافت فایل اصل مقاله7,652,185
Zarifi, Fariba, Rafiee, Shima, Borhan-Haghighi, Maryam, Talaei-Khozani, Tahereh, Aliabadi, Elham. (1396). Lectin Histochemistry Showed a Heterogeneous Population of Cells Among Human Mesenchymal Stem Cells Isolated From Adipose Tissue. سامانه مدیریت نشریات علمی, 3(2), 77-84. doi: 10.18869/nrip.jamsat.3.2.77
Fariba Zarifi; Shima Rafiee; Maryam Borhan-Haghighi; Tahereh Talaei-Khozani; Elham Aliabadi. "Lectin Histochemistry Showed a Heterogeneous Population of Cells Among Human Mesenchymal Stem Cells Isolated From Adipose Tissue". سامانه مدیریت نشریات علمی, 3, 2, 1396, 77-84. doi: 10.18869/nrip.jamsat.3.2.77
Zarifi, Fariba, Rafiee, Shima, Borhan-Haghighi, Maryam, Talaei-Khozani, Tahereh, Aliabadi, Elham. (1396). 'Lectin Histochemistry Showed a Heterogeneous Population of Cells Among Human Mesenchymal Stem Cells Isolated From Adipose Tissue', سامانه مدیریت نشریات علمی, 3(2), pp. 77-84. doi: 10.18869/nrip.jamsat.3.2.77
Zarifi, Fariba, Rafiee, Shima, Borhan-Haghighi, Maryam, Talaei-Khozani, Tahereh, Aliabadi, Elham. Lectin Histochemistry Showed a Heterogeneous Population of Cells Among Human Mesenchymal Stem Cells Isolated From Adipose Tissue. سامانه مدیریت نشریات علمی, 1396; 3(2): 77-84. doi: 10.18869/nrip.jamsat.3.2.77

Lectin Histochemistry Showed a Heterogeneous Population of Cells Among Human Mesenchymal Stem Cells Isolated From Adipose Tissue

Journal of Advanced Medical Sciences and Applied Technologies
مقاله 4، دوره 3، شماره 2، شهریور 2017، صفحه 77-84    اصل مقاله (938.58 K)
نوع مقاله: Original Articles
شناسه دیجیتال (DOI): 10.18869/nrip.jamsat.3.2.77
نویسندگان
Fariba Zarifi1؛ Shima Rafiee2؛ Maryam Borhan-Haghighi1؛ Tahereh Talaei-Khozani1؛ Elham Aliabadi* 1
1Department of Anatomy, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
2Student Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
چکیده
Objectives: Adipose tissue as an appropriate source of Mesenchymal Stem Cells (MSCs) has the potential to differentiate into multiple lineages. Glycoconjugates content of the MSCs can be considered as biomarkers in self-renewal, pluripotency and differentiation processes. In this study, the lectin profile of MSCs isolated from adipose tissue was detected and according to that, a subpopulation was determined. Materials & Methods: MSCs were isolated from adipose tissue by explanting of the tissue pieces. The FITC-conjugated lectins, WGA, UEA, PNA, BSA and PWM were used to detect the terminal sugar residues. The cells were then counterstained with DAPI. The intensity of the reaction was evaluated by ImageJ software. The cells were also stained with PAS method.Results: MSCs were reacted with all lectins with different intensity of the reactions. The cells reacted with WGA, UEA, and BSA “strongly” and with PWM “moderately” and with PNA with “weak” intensity. The morphological analysis of the isolated MSCs revealed the existence of the two different cell types in the cultures. Two types of cells were detected according to nucleus size and lectin reactivity. The cells with large nuclei constitute 20.62% of the total cells and stained significant more intensity by UEA and less intense with PWM (both P=0.014) and PNA (P=0.044). Flow cytometry with CD34 shows that these large cells were not endothelial cells. Conclusion: The MSCs derived from adipose tissue seem to be a heterogeneous populations and lectin profile of the cells showed that they are different in the expression of the glycoconjugates. 
کلیدواژه‌ها
Adipose tissue؛ Mesenchymal stem cell؛ Lectin؛ Glycoconjugate
مراجع
  1. Kern S, Eichler H, Stoeve J, Klüter H, Bieback K. Comparative analysis of mesenchymal stem cells from bone marrow, umbilical cord blood, or adipose tissue. Stem Cells. 2006; 24(5):1294–301. doi: 10.1634/stemcells.2005-0342
  2. Dominici M, Paolucci P, Conte P, Horwitz EM. Heterogeneity ofmultipotent mesenchymal stromal cells: From stromal cells to stem cells and vice versa. Transplantation. 2009; 87:36–42. doi: 10.1097/tp.0b013e3181a283ee
  3. Banas A, Teratani T, Yamamoto Y, Tokuhara M, Takeshita F, Quinn G, et al. Adipose tissue-derived mesenchymal stem cells as a source of human hepatocytes. Hepatology. 2007; 46(1):219–28. doi: 10.1002/hep.21704
  4. Kawasaki-Oyama RS, Braile DM, Caldas HC, Leal JCF, Goloni-Bertollo EM, Pavarino-Bertelli ÉC, et al. [Blood mesenchymal stem cell culture from the umbilical cord with and without Ficoll-Paque density gradient method (Portuguese)]. Brazilian Journal of Cardiovascular Surgery. 2008; 23(1):29-34. PMID: 18719825
  5. Talaei-Khozani T, Vojdani Z, Aliabadi E. A study of the glycoconjugates distribution of umbilical cord; a lectin histochemical study. Journal of Infertility and Reproductive Biology. 2013; 1(1):7-11.
  6. Lavrov AV, Smirnikhina SA. Nuclear heterogeneity and proliferation activity of human adipose derived MSC-like cells. Cell and Tissue Biology. 2010; 4(5):452–6. doi: 10.1134/s1990519x1005007x
  7. Baer PC, Geiger H. Adipose-derived mesenchymal stromal/stem cells: Tissue localization, characterization, and heterogeneity. Stem Cells International. 2012; 2012:1–11. doi: 10.1155/2012/812693
  8. Mescher A. Junqueira’s basic histology: Text and atlas. New York: Mcgraw-hill; 2013.
  9. Karsten U, Goletz S. What makes cancer stem cell markers different? Springer Plus. 2013; 2(1):301. doi: 10.1186/2193-1801-2-301
  10. Yagi H, Kato K. Functional roles of glycoconjugates in the maintenance of stemness and differentiation process of neural stem cells. Glycoconjugate Journal. 2016; 1-7. doi: 10.1007/s10719-016-9707-x
  11. Rosenman S, Gallatin W. Cell surface glycoconjugates in intercellular and cell-substratum interactions. Seminars in cancer biology. 1991; 2(6):357-66. PMID: 1810465
  12. Sharon N. Lectins: Carbohydrate-specific reagents and biological recognition molecules. Journal of Biological Chemistry. 2007; 282(5):2753–64. doi: 10.1074/jbc.x600004200
  13. Kang J, Park HM, Kim YW, Kim Y, Varghese S, Seok HK, et al. Control of mesenchymal stem cell phenotype and differentiation depending on cell adhesion mechanism. European Cells and Materials. 2014; 28:387–403. doi: 10.22203/ecm.v028a27
  14. Talaei-Khozani T, Monsefi M, Ghasemi M. Lectins influence chondrogenesis and osteogenesis in limb bud mesenchymal cells. Glycoconjugate Journal. 2011; 28(2):89–98. doi: 10.1007/s10719-011-9326-5
  15. Choi JH, Lyu SY, Lee HJ, Jung J, Park WB, Kim GJ. Korean mistletoe lectin regulates self-renewal of placenta-derived mesenchymal stem cells via autophagic mechanisms. Cell Proliferation. 2012; 45(5):420–9. doi: 10.1111/j.1365-2184.2012.00839.x
  16. Diogo MM, Da Silva CL, Cabral JM. Separation technologies for stem cell bioprocessing. Biotechnology and Bioengineering. 2012; 109(11):2699-709. doi: 10.1002/bit.24706
  17. Griesche N, Luttmann W, Luttmann A, Stammermann T, Geiger H, Baer PC. A simple modification of the separation method reduces heterogeneity of adipose-derived stem cells. Cells Tissues Organs. 2010; 192(2):106–15. doi: 10.1159/000289586
  18. Rada T, Reis RL, Gomes ME. Distinct stem cells subpopulations isolated from human adipose tissue exhibit different chondrogenic and osteogenic differentiation potential. Stem Cell Reviews and Reports. 2010; 7(1):64–76. doi: 10.1007/s12015-010-9147-0
  19. Anderson P, Carrillo-Galvez AB, Garcia-Perez A, Cobo M, Martin F. CD105 (Endoglin)-negative murine mesenchymal stromal cells define a new multipotent subpopulation with distinct differentiation and im-munomodulatory capacities. PLoS ONE. 2013; 8(10):e76979. doi: 10.1371/journal.pone.0076979
  20. Singh R. Peanut lectin stimulates proliferation of colon cancer cells by interaction with glycosylated CD44v6 isoforms and consequential activation of c-Met and MAPK: Functional implications for disease-associated glycosylation changes. Glycobiology. 2006; 16(7):594–601. doi: 10.1093/glycob/cwj108
  21. Zayed S, Gaafar T, Samy R, Sabry D, Nasr A, Maksoud FA. Production of endothelial progenitor cells obtained from human Wharton's jelly using different culture conditions. Biotechnic & Histochemistry. 2016; 91(8):532-9. doi: 10.1080/10520295.2016.1250284
  22. Song E, Lu CW, Fang LJ, Yang W. Culture and identification of endothelial progenitor cells from human umbilical cord blood. International Journal of Ophthalmology. 2010; 3(1): 49–53. doi: 10.3980/j.issn.2222-3959.2010.01.11
  23. Zhou L, Xia J, Qiu X, Wang P, Jia R, Chen Y, et al. in vitro evaluation of endothelial progenitor cells from adipose tissue as potential angiogenic cell sources for bladder angiogen-esis. PLOS ONE. 2015; 10(2):0117644. doi: 10.1371/journal.pone.0117644
  24. Mandai M, Ikeda H, Jin ZB, Iseki K, Ishigami C, Takahashi M. Use of lectins to enrich mouse es-derived retinal progenitor cells for the purpose of transplantation therapy. Cell Transplantation. 2010; 19(1):9–19. doi: org/10.3727/096368909x476599
  25. Astori G, Vignati F, Bardelli S, Tubio M, Gola M, Albertini V, et al. “In vitro” and multicolor phenotypic characterization of cell subpopulations identified in fresh human adipose tissue stromal vascular fraction and in the derived mesenchymal stem cells. Journal of Translational Medicine. 2007; 5(1):55. doi: 10.1186/1479-5876-5-55
آمار
تعداد مشاهده مقاله: 1,863
تعداد دریافت فایل اصل مقاله: 326


سامانه مدیریت نشریات علمی. قدرت گرفته از سیناوب